NO950849D0 - Derivatives of valproin and 2-valproic acid amides and use as anticonvulsants - Google Patents
Derivatives of valproin and 2-valproic acid amides and use as anticonvulsantsInfo
- Publication number
- NO950849D0 NO950849D0 NO950849A NO950849A NO950849D0 NO 950849 D0 NO950849 D0 NO 950849D0 NO 950849 A NO950849 A NO 950849A NO 950849 A NO950849 A NO 950849A NO 950849 D0 NO950849 D0 NO 950849D0
- Authority
- NO
- Norway
- Prior art keywords
- valproin
- anticonvulsants
- derivatives
- acid amides
- valproic acid
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/45—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
- C07C233/46—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
- C07C233/49—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to a carbon atom of an acyclic unsaturated carbon skeleton
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/08—Antiepileptics; Anticonvulsants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/45—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups
- C07C233/46—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom
- C07C233/47—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by carboxyl groups with the substituted hydrocarbon radical bound to the nitrogen atom of the carboxamide group by an acyclic carbon atom having the carbon atom of the carboxamide group bound to a hydrogen atom or to a carbon atom of an acyclic saturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
- C07C237/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
- C07C237/22—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
- C07C255/24—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the same saturated acyclic carbon skeleton
- C07C255/29—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the same saturated acyclic carbon skeleton containing cyano groups and acylated amino groups bound to the carbon skeleton
Abstract
A compound having the structure: <IMAGE> wherein R1, R2, and R3 are independently the same or different and are hydrogen, a C1-C6 alkyl group, an aralkyl group, or an aryl group, and n is an integer which is greater than or equal to 0 and less than or equal to 3. Also provided are a compound containing a 2-valproenoic moiety, pharmaceutical compositions comprising these compounds, and methods of using them for the effective treatment of epilepsy and other neurological disorders.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/088,074 US5585358A (en) | 1993-07-06 | 1993-07-06 | Derivatives of valproic acid amides and 2-valproenoic acid amides, method of making and use thereof as anticonvulsant agents |
PCT/US1994/007498 WO1995001956A1 (en) | 1993-07-06 | 1994-07-06 | Derivatives of valproic and 2-valproenoic acid amides and use as anticonvulsants |
Publications (3)
Publication Number | Publication Date |
---|---|
NO950849D0 true NO950849D0 (en) | 1995-03-03 |
NO950849L NO950849L (en) | 1995-04-26 |
NO308792B1 NO308792B1 (en) | 2000-10-30 |
Family
ID=22209256
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO950849A NO308792B1 (en) | 1993-07-06 | 1995-03-03 | Derivatives of valproic acid and 2-valproic acid amides, their pharmaceutical composition and their use in the preparation of a pharmaceutical preparation |
Country Status (23)
Country | Link |
---|---|
US (1) | US5585358A (en) |
EP (1) | EP0659174B1 (en) |
JP (1) | JP3856464B2 (en) |
KR (1) | KR100362424B1 (en) |
CN (2) | CN100457720C (en) |
AT (1) | ATE176664T1 (en) |
AU (1) | AU673766B2 (en) |
CA (1) | CA2143636C (en) |
CZ (1) | CZ288328B6 (en) |
DE (1) | DE69416501T2 (en) |
DK (1) | DK0659174T3 (en) |
ES (1) | ES2131207T3 (en) |
GR (1) | GR3030183T3 (en) |
HK (1) | HK1055726A1 (en) |
HU (1) | HU221968B1 (en) |
IL (3) | IL110216A (en) |
NO (1) | NO308792B1 (en) |
NZ (1) | NZ269643A (en) |
RO (1) | RO113461B1 (en) |
RU (1) | RU2140904C1 (en) |
SK (1) | SK282456B6 (en) |
WO (1) | WO1995001956A1 (en) |
ZA (1) | ZA944884B (en) |
Families Citing this family (44)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4326465A1 (en) * | 1993-01-20 | 1995-02-09 | Thomae Gmbh Dr K | Amino acid derivatives, pharmaceutical compositions containing these compounds and process for their preparation |
US6028102A (en) * | 1998-02-24 | 2000-02-22 | Yissum Research Development Company Of The Hebrew University Of Jerusalem | Anticonvulsant drugs and pharmaceutical compositions thereof |
CN1251758C (en) * | 2000-07-21 | 2006-04-19 | 特瓦制药工业有限公司 | Use of derivatives of valproic acid and 2-valproenic acid amides for treatment of mania in bipolar disorder |
US6323365B1 (en) * | 2000-07-28 | 2001-11-27 | Yissum Research Development Company Of The Hebrew University Of Jerusalem | Active derivative of valproic acid for the treatment of neurological and psychotic disorders and a method for their preparation |
AU8830801A (en) * | 2000-08-17 | 2002-02-25 | Teva Pharma | Use of derivatives of valproic acid amides and 2-valproenic acid amides for the treatment or prevention of pain and/or headache disorders |
US6521790B2 (en) | 2000-11-01 | 2003-02-18 | Abbott Laboratories | Alkynyl amides and their therapeutic applications |
PE20020575A1 (en) | 2000-11-01 | 2002-06-25 | Abbott Lab | ALKYNYLAMIDES AND THERAPEUTIC APPLICATIONS OF THE SAME |
DE60120104T2 (en) | 2001-03-20 | 2006-09-21 | Schwarz Pharma Ag | New use of peptide compounds in the treatment of non-neuropathic inflammatory pain |
EP1243263B1 (en) * | 2001-03-21 | 2002-11-27 | Schwarz Pharma Ag | Novel use of a peptide class of compound for treating allodynia or other different types of chronic or phantom pain |
WO2003000654A1 (en) * | 2001-06-26 | 2003-01-03 | Yissum Research Development Company Of The Hebrew University Of Jerusalem | Valproyltaurinamide derivatives as anticonvulsant and cns active agents |
WO2003078448A1 (en) | 2002-03-13 | 2003-09-25 | Signum Biosciences, Inc. | Modulation of protein methylation and phosphoprotein phosphate |
EP1537074B1 (en) * | 2002-09-04 | 2019-02-27 | Merck Canada Inc. | Cathepsin cysteine protease inhibitors |
US20040175423A1 (en) * | 2003-02-05 | 2004-09-09 | Daniella Licht | Sustained release formulation of N- (2-propylpentanoyl) glycinamide and related compounds |
WO2004071424A2 (en) * | 2003-02-05 | 2004-08-26 | Teva Pharmaceutical Industries, Ltd. | Immediate release formulation of n-(2-propylpentanoyl)glycinamide |
IL157751A0 (en) * | 2003-02-28 | 2004-03-28 | Yissum Res Dev Co | New amide derivatives of 2,2,3,3-tetramethylcyclopropane carboxylic acid, a method for their synthesis and pharmaceutical compositions containing them |
KR20060111524A (en) * | 2003-12-02 | 2006-10-27 | 쉬바르츠파르마에이지 | Novel use of peptide compounds for treating central neuropathic pain |
US20060009384A1 (en) * | 2003-12-05 | 2006-01-12 | David Rudd | Novel use of peptide compounds for treating status epilepticus or related conditions |
US20070042969A1 (en) * | 2004-03-26 | 2007-02-22 | Srz Properties, Inc. | Combination therapy for pain in painful diabetic neuropathy |
EP1579858A1 (en) * | 2004-03-26 | 2005-09-28 | Schwarz Pharma Ag | Novel use of peptide compounds for treating pain in painful diabetic neuropathy |
US20100256179A1 (en) * | 2004-03-26 | 2010-10-07 | Ucb Pharma Gmbh | Combination therapy for pain in painful diabetic neuropathy |
CN1950101B (en) * | 2004-04-16 | 2011-03-30 | 舒沃茨药物股份公司 | Use of peptidic compounds for the prophylaxis and treatment of chronic headache |
EP1604655A1 (en) * | 2004-06-09 | 2005-12-14 | Schwarz Pharma Ag | Novel use of peptide compounds for treating pain in trigeminal neuralgia |
US20060025477A1 (en) * | 2004-07-22 | 2006-02-02 | Artman Linda D | Analogs of isovaleramide, a pharmaceutical composition including the same, and a method of treating central nervous system conditions or diseases |
WO2006021412A2 (en) * | 2004-08-27 | 2006-03-02 | Schwarz Pharma Ag | Use of peptide compounds for treating bone cancer pain, chemotherapy-and nucleoside-induced pain |
EP1642889A1 (en) * | 2004-10-02 | 2006-04-05 | Schwarz Pharma Ag | Improved synthesis scheme for lacosamide |
US20060252749A1 (en) * | 2005-01-28 | 2006-11-09 | Srz Properties, Inc. | Lacosamide for add-on therapy of psychosis |
US7923041B2 (en) | 2005-02-03 | 2011-04-12 | Signum Biosciences, Inc. | Compositions and methods for enhancing cognitive function |
US8221804B2 (en) | 2005-02-03 | 2012-07-17 | Signum Biosciences, Inc. | Compositions and methods for enhancing cognitive function |
US20070043120A1 (en) * | 2005-08-18 | 2007-02-22 | Bettina Beyreuther | Therapeutic combination for painful medical conditions |
EP1754476A1 (en) * | 2005-08-18 | 2007-02-21 | Schwarz Pharma Ag | Lacosamide (SPM 927) for treating myalgia, e.g. fibromyalgia |
EP1928807A4 (en) * | 2005-09-02 | 2011-05-04 | Picobella Llc | Oncogenic regulatory rnas for diagnostics and therapeutics |
AU2006287378A1 (en) * | 2005-09-07 | 2007-03-15 | Braincells, Inc. | Modulation of neurogenesis by HDac inhibition |
US7459280B2 (en) * | 2006-02-27 | 2008-12-02 | Picobella, Llc | Methods for diagnosing and treating kidney cancer |
AR061476A1 (en) | 2006-06-15 | 2008-08-27 | Sanol Arznei Schwarz Gmbh | PHARMACEUTICAL COMPOSITION WITH SYNERGIC ANTI-CONVULSIVE EFFECT |
CN101466390B (en) | 2006-06-15 | 2014-03-12 | 优时比制药有限公司 | Pharmaceutical composition with synergistic anticonvulsant effect |
EP1873527A1 (en) * | 2006-06-30 | 2008-01-02 | Schwarz Pharma Ag | Method for identifying CRMP modulators |
US20080267977A1 (en) * | 2007-04-26 | 2008-10-30 | Friedrich-Alexander University Of Erlangen-Nuremberg | Combined immunological agent and sensitizing agent for the treatment of cancer |
ES2326355B1 (en) * | 2008-02-25 | 2010-08-10 | Centro Atlantico Del Medicamento, S.A. | ACID 1- (DI-N-PROPILACETILAMINOMETIL) -CICLOHEXILACETICO. |
AU2009239430B2 (en) | 2008-04-21 | 2015-01-22 | Signum Biosciences, Inc. | Compounds, compositions and methods for making the same |
EP2468261A1 (en) | 2010-12-02 | 2012-06-27 | UCB Pharma GmbH | Formulation of lacosamide |
EP3842450A1 (en) | 2015-10-23 | 2021-06-30 | Eureka Therapeutics, Inc. | Antibody/t-cell receptor chimeric constructs and uses thereof |
CN110662547A (en) | 2017-04-26 | 2020-01-07 | 优瑞科生物技术公司 | Cells expressing chimeric activating receptors and chimeric stimulating receptors and uses thereof |
CN112972449B (en) * | 2019-12-18 | 2023-03-21 | 四川科瑞德制药股份有限公司 | Pharmaceutical composition with high safety and preparation method thereof |
WO2021245503A1 (en) * | 2020-06-05 | 2021-12-09 | Cellix Bio Private Limited | Process for the preparation of eflornithine derivatives and their pharmaceutical acceptable salts thereof |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3050800C2 (en) * | 1979-03-22 | 1989-06-22 | Continental Pharma Inc., Bruessel/Bruxelles, Be | |
FR2489319A1 (en) * | 1980-08-27 | 1982-03-05 | Clin Midy | DERIVATIVES OF AMINO-4 BUTYRIC ACID AND MEDICAMENTS, PARTICULARLY ACTIVE ON THE CENTRAL NERVOUS SYSTEM, CONTAINING |
BE885303A (en) * | 1980-09-19 | 1981-03-19 | Continental Pharma | GLYCINAMIDES |
DK373383A (en) * | 1982-08-20 | 1984-02-21 | Midit | PROCEDURE FOR THE PREPARATION OF OMEGA AMINO ACID DERIVATIVES |
US4913906B1 (en) * | 1985-02-28 | 2000-06-06 | Yissum Res Dev Co | Controlled release dosage form of valproic acid |
IT1190133B (en) * | 1986-06-19 | 1988-02-10 | Chiesi Farma Spa | VALPROIC ACID AND (E) -2-VALPROENOIC ACID DERIVATIVES, PROCEDURE FOR THEIR PREPARATION AND RELATED PHARMACEUTICAL COMPOSITIONS |
FR2620447B1 (en) * | 1987-09-15 | 1990-01-26 | Sanofi Sa | PROCESS FOR THE PREPARATION OF DI-N-PROPYLACETONITRILE |
-
1993
- 1993-07-06 US US08/088,074 patent/US5585358A/en not_active Expired - Lifetime
-
1994
- 1994-07-05 IL IL11021694A patent/IL110216A/en not_active IP Right Cessation
- 1994-07-05 IL IL13389194A patent/IL133891A/en not_active IP Right Cessation
- 1994-07-06 ZA ZA944884A patent/ZA944884B/en unknown
- 1994-07-06 DE DE69416501T patent/DE69416501T2/en not_active Expired - Lifetime
- 1994-07-06 AU AU73968/94A patent/AU673766B2/en not_active Ceased
- 1994-07-06 CN CNB021053588A patent/CN100457720C/en not_active Expired - Fee Related
- 1994-07-06 SK SK395-95A patent/SK282456B6/en not_active IP Right Cessation
- 1994-07-06 WO PCT/US1994/007498 patent/WO1995001956A1/en active IP Right Grant
- 1994-07-06 CA CA002143636A patent/CA2143636C/en not_active Expired - Fee Related
- 1994-07-06 HU HU9500503A patent/HU221968B1/en not_active IP Right Cessation
- 1994-07-06 EP EP94923915A patent/EP0659174B1/en not_active Expired - Lifetime
- 1994-07-06 RO RO95-00475A patent/RO113461B1/en unknown
- 1994-07-06 ES ES94923915T patent/ES2131207T3/en not_active Expired - Lifetime
- 1994-07-06 JP JP50409795A patent/JP3856464B2/en not_active Expired - Fee Related
- 1994-07-06 RU RU95108243A patent/RU2140904C1/en not_active IP Right Cessation
- 1994-07-06 KR KR1019950700884A patent/KR100362424B1/en not_active IP Right Cessation
- 1994-07-06 CZ CZ1995853A patent/CZ288328B6/en not_active IP Right Cessation
- 1994-07-06 DK DK94923915T patent/DK0659174T3/en active
- 1994-07-06 AT AT94923915T patent/ATE176664T1/en not_active IP Right Cessation
- 1994-07-06 NZ NZ269643A patent/NZ269643A/en not_active IP Right Cessation
- 1994-07-06 CN CN94190471A patent/CN1106379C/en not_active Expired - Fee Related
-
1995
- 1995-03-03 NO NO950849A patent/NO308792B1/en not_active IP Right Cessation
-
1999
- 1999-05-10 GR GR990401269T patent/GR3030183T3/en unknown
-
2000
- 2000-01-05 IL IL13389100A patent/IL133891A0/en unknown
-
2003
- 2003-11-10 HK HK03108127.6A patent/HK1055726A1/en not_active IP Right Cessation
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM1K | Lapsed by not paying the annual fees |